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0.0 - 5.0 years
2 - 5 Lacs
Ankleshwar
Work from Office
Vacancy as per following 01. QA Officer / Executive : Required Candidates who have completed B.Pharm / M.Pharm for QA Department and must have experience of QMS and IPQA in Pharma formulation plant. 02. QA Officer / Executive : Required Candidates who have completed B.Pharm / M.Pharm / M.Sc. for QA Department and must have experience of QA in QC Dept. in Pharma formulation plant. 03. Production Officer / Executive : Required Candidates who have completed B.Pharm / M.Pharm for Production Manufacturing Department and must have experience of Production Dept. in Pharma formulation plant.
Posted 2 weeks ago
10 - 17 years
10 - 20 Lacs
Ahmedabad
Work from Office
We are hiring for a Green Field Projects at Amneal , Ahmedabad. Following is the JD : Key Responsibilities : Lead QA operations related to Qualification & Validation, including Cleaning Validation, Process Performance Qualification (PPQ), and Computer System Validation (CSV). Develop and implement Validation Master Plans (VMP), Contamination Control Strategies, and Quality Risk Management (QRM) frameworks. Ensure qualification and validation of manufacturing equipment, utilities, and computerized systems to meet regulatory requirements. Drive regulatory inspection readiness, acting as SME for audits including USFDA, EMA, ANVISA, and WHO. Implement and optimize QMS using a risk-based approach, ensuring continuous monitoring and integration of compliance standards. Oversee execution of large-scale validation projects, such as Green Field Injectable facilities, and ensure regulatory approval readiness. Collaborate cross-functionally with Quality, Engineering, Production, and Regulatory Affairs teams for the successful and timely delivery of validation-related initiatives. Promote lean validation practices and continuous improvement strategies to enhance operational efficiency and regulatory compliance. Mentor, develop, and manage a high-performing QA validation team in a cross-cultural, fast-paced environment. Key Requirements : Education : Bachelors or Masters degree in Pharmacy, Chemistry, or related life sciences field. Experience : Minimum 15 years of experience in QA with strong specialization in Qualification & Validation within pharmaceutical manufacturing. Proven experience in injectable/sterile manufacturing environments is highly desirable. Hands-on experience in handling international regulatory audits and validations across FDA, EMA, and ANVISA-regulated markets. Technical Skills : Expertise in Cleaning Validation, PPQ, CSV, QRM, and VMP development. Strong command of GxP and global regulatory guidelines. Proficient in developing and managing QMS with focus on compliance and risk management. Leadership Skills : Demonstrated ability to lead cross-functional teams, influence stakeholders, and manage complex projects under tight timelines. Strong communication, decision-making, and coaching capabilities. Preferred Attributes : Green Field project experience, especially in injectables. Recognized as an SME in QA Validation. Familiarity with modern digital QA tools or systems is an added advantage. Interested candidate can share CV at bhuvneshwari.rathore@amneal.com
Posted 1 month ago
11 - 15 years
11 - 15 Lacs
Chennai
Work from Office
Greetings!!! We are seeking for a QA Validation (Dy Manager/ Manager )_Injectables for a Pharma Company at Chennai Location. Job Responsibilities: Responsible to ensures the quality and compliance of injectable products through validation and qualification activities, reviewing documentation, and conducting audits, all while adhering to GMP and regulatory requirements. Key Responsibilities: Validation and Qualification: Executes and reviews qualification/re-qualification and validation activities for equipment, systems, facilities, and plant utilities. Prepares and reviews validation/qualification protocols and reports. Conducts sampling activities as per protocols, including process and cleaning validation. Ensures all equipment, systems, and processes are validated and qualified according to GMP and regulatory standards. Documentation and Review: Reviews and approves validation lifecycle documentation (e.g., URS, DQ, FAT, SAT, IQ, OQ, PQ, PV) protocols and reports. Maintains validation registers. Reviews and approves validation deviations. Ensures all documentation is complete and accurate. Quality Assurance: Conducts quality assurance audits and inspections. Identifies and addresses potential quality issues. Ensures adherence to GMP and regulatory requirements. Participates in investigations and CAPA activities. Interested Candidates Kindly share your updated cv to khyati@bvrpc.com
Posted 2 months ago
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